A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3556108



Internal ID18854389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35232188..35475416hg38UCSC Ensembl
Innerchr16:34466559..34709787hg19UCSC Ensembl
Innerchr16:34324060..34567288hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38243229
hg19243229
hg18243229
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057261
Supporting Variants
Samples
Known GenesLOC283914
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3556108
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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